Mouridsen Henning T, Robert Nicholas J
Department of Oncology, Rigshospitalet, 9 Blegdamsvej, Copenhagen DK-2100, Denmark.
Eur J Cancer. 2005 Aug;41(12):1678-89. doi: 10.1016/j.ejca.2004.10.020. Epub 2004 Nov 25.
For endocrine therapy of hormone-sensitive advanced breast cancer in postmenopausal women, the third-generation aromatase inhibitors, letrozole, anastrozole, and exemestane, are effective both as alternatives to tamoxifen in first-line treatment and following first-line tamoxifen failure. These three agents are currently being evaluated as adjuvant therapy of early breast cancer, again relative to the standard, tamoxifen. Three treatment strategies are under investigation: replacement of tamoxifen as adjuvant therapy for 5 years (early adjuvant therapy); sequencing of tamoxifen before or after an aromatase inhibitor during the first 5 years (early sequential adjuvant therapy); or following 5 years of tamoxifen (extended adjuvant therapy). Results of the first early adjuvant trial (Arimidex, Tamoxifen Alone or in Combination [ATAC]) demonstrated that anastrozole was significantly more effective than tamoxifen in reducing the risk of disease recurrence. Two trials sequencing 2-3 years of an aromatase inhibitor after 2-3 years of tamoxifen have also reported results. A large trial (International Collaborative Cancer Group [ICCG] trial 96) found switching to exemestane to be significantly superior to continuing on tamoxifen in disease-free survival, and in a small study (Italian Tamoxifen Arimidex [ITA] trial), similarly sequencing anastrozole after tamoxifen significantly reduced the hazard of recurrence compared with remaining on tamoxifen. Extended adjuvant therapy with 5 years of letrozole versus placebo following 5 years of tamoxifen was evaluated in the MA.17 trial. Compared with placebo, letrozole resulted in a significant improvement in disease-free survival that was irrespective of whether patients had lymph node-positive or -negative tumours. Results of these four trials emphasise the important role of aromatase inhibitors in the adjuvant setting, yet the optimal approach still needs to be defined. A number of trials further evaluating the three adjuvant treatment strategies are ongoing.
对于绝经后女性激素敏感性晚期乳腺癌的内分泌治疗,第三代芳香化酶抑制剂来曲唑、阿那曲唑和依西美坦,在一线治疗中作为他莫昔芬的替代药物以及在一线他莫昔芬治疗失败后均有效。目前正在评估这三种药物相对于标准药物他莫昔芬作为早期乳腺癌辅助治疗的效果。正在研究三种治疗策略:替代他莫昔芬作为5年辅助治疗(早期辅助治疗);在最初5年中他莫昔芬之前或之后序贯使用芳香化酶抑制剂(早期序贯辅助治疗);或在他莫昔芬治疗5年后(延长辅助治疗)。首个早期辅助试验(阿那曲唑、他莫昔芬单药或联合应用[ATAC]试验)的结果表明,阿那曲唑在降低疾病复发风险方面显著优于他莫昔芬。两项在2 - 3年他莫昔芬治疗后序贯使用2 - 3年芳香化酶抑制剂的试验也报告了结果。一项大型试验(国际癌症协作组[ICCG]试验96)发现,转换为依西美坦在无病生存方面显著优于继续使用他莫昔芬,并且在一项小型研究(意大利他莫昔芬阿那曲唑[ITA]试验)中,同样在他莫昔芬之后序贯使用阿那曲唑与继续使用他莫昔芬相比,显著降低了复发风险。MA.17试验评估了在5年他莫昔芬治疗后使用5年来曲唑与安慰剂进行延长辅助治疗的效果。与安慰剂相比,来曲唑在无病生存方面有显著改善,无论患者肿瘤为淋巴结阳性还是阴性。这四项试验的结果强调了芳香化酶抑制剂在辅助治疗中的重要作用,但最佳方法仍有待确定。一些进一步评估这三种辅助治疗策略的试验正在进行中。